An Open-Circuit Voltage and Power Conversion Efficiency Study of Fullerene Ternary Organic Solar Cells Based on Oligomer/Oligomer and Oligomer/Polymer.

Macromol Rapid Commun

State Key Laboratory of Luminescent Materials and Devices, Institute of Polymer Optoelectronic Materials and Devices, South China University of Technology, Guangzhou, 510640, China.

Published: July 2017

Variations in the open-circuit voltage (V ) of ternary organic solar cells are systematically investigated. The initial study of these devices consists of two electron-donating oligomers, S2 (two units) and S7 (seven units), and the electron-accepting [6,6]-phenyl C71 butyric acid methyl ester (PC BM) and reveals that the V is continuously tunable due to the changing energy of the charge transfer state (E ) of the active layers. Further investigation suggests that V is also continuously tunable upon change in E in a ternary blend system that consists of S2 and its corresponding polymer (P11):PC BM. It is interesting to note that higher power conversion efficiencies can be obtained for both S2:S7:PC BM and S2:P11:PC BM ternary systems compared with their binary systems, which can be ascribed to an improved V due to the higher E and an improved fill factor due to the improved film morphology upon the incorporation of S2. These findings provide a new guideline for the future design of conjugated polymers for achieving higher performance of ternary organic solar cells.

Download full-text PDF

Source
http://dx.doi.org/10.1002/marc.201700090DOI Listing

Publication Analysis

Top Keywords

ternary organic
12
organic solar
12
solar cells
12
open-circuit voltage
8
power conversion
8
continuously tunable
8
ternary
5
voltage power
4
conversion efficiency
4
efficiency study
4

Similar Publications

The discovery of new structures is very important for metal-organic framework (MOF) adsorbents and their application in gas separation, where the design of ligands and the selection of metal ions play a decisive role. Herein, we synthesized two isoreticular Zn-MOFs, UPC-250 and UPC-251, composed of imidazole-based tricarboxylic acid ligands and binuclear zinc clusters. The pore environment was regulated via modifying fluorine atoms at different positions of ligands, and one-step purification of ethylene from acetylene/ethylene/ethane ternary mixture was realized in UPC-251.

View Article and Find Full Text PDF

Construction of ternary heterojunction photocatalyst CuCl(OH)/In/InO for boosted photocatalytic CO reduction performance.

Dalton Trans

January 2025

College of Life Sciences, School of Chemical Engineering, Key Laboratory of Green Catalysis of Jiangxi Education Institutes, Jiangxi Normal University, Nanchang 330022, China.

The photocatalytic conversion of CO and HO into useful chemicals or fuels over semiconductor photocatalysts is regarded as a promising technology to address the problems of global warming and energy exhaustion. However, inefficient photo-absorption and slow charge dynamics limit the CO photoreduction efficiency. Here, a ternary heterojunction photocatalyst, CuCl(OH)/In/InO (Cu H IO), with an intimate interface is obtained a hydrogen chemical reduction approach followed by hydrolysis reaction, where In species can be produced on the surface of InO from the hydrogen chemical reaction with a calcining temperature of over 500 °C.

View Article and Find Full Text PDF

Introduction of a guest component into the active layer is a simple yet effective approach to enhance the performance of organic solar cells (OSCs). Despite various guest components successfully employed in the OSCs, efficient guest components require deliberate design and ingenious inspiration, which still remains a big challenge for developing high performance OSCs. In this work, we propose a concept of "structural gene" engineering to create a new "double-gene" small molecule (L-DBDD) by simply combining the structures of both donor PM6 and acceptor L8-BO.

View Article and Find Full Text PDF

Efficient and Robust Europium(III)-Based Hybrid Lanthanide Scintillators for Advanced X-ray Imaging.

Angew Chem Int Ed Engl

January 2025

South China Normal University, Guangdong Provincial Key Laboratory of Quantum Engineering and Quantum Material, School of Physics and Telecommunication Engineering, Panyu University Mega Center, 510006, Guangzhou, CHINA.

Scintillators that convert ionizing radiation into low-energy photons are essential for medical diagnostics and industrial inspections. Despite advances in X-ray scintillators, challenges remain in achieving high efficiency, environmental compatibility, stability, and flexibility. Here, we present experimental investigations of a new type of europium(III)-based hybrid ternary complex scintillators for improved X-ray detection and imaging.

View Article and Find Full Text PDF

A theoretical comparison of different third component content in ternary organic solar cells.

Phys Chem Chem Phys

January 2025

School of Chemistry and Environmental Engineering, Changchun University of Science and Technology, Jilin Provincial Science and Technology Innovation Center of Optical Materials and Chemistry, Jilin Provincial International Joint Research Center of Photo-functional Materials and Chemistry, Changchun, 130022, China.

Article Synopsis
  • Ternary solar cells are being developed to enhance the efficiency of organic solar cells by adding a third component, though the relationship between morphology and power conversion efficiency (PCE) is not fully understood.
  • Researchers constructed two ternary active layers with different Y7 component contents and investigated how these variations affect PCE through theoretical calculations.
  • The study reveals that increasing Y7 content shifts the stacking patterns in the active layer, influencing charge separation and enhancing PCE, while also laying groundwork for future experiments involving non-fullerene materials.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!